Compounds > valine

valine and Inclusion Body Myopathy, Sporadic

valine has been researched along with Inclusion Body Myopathy, Sporadic in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akuta, N; Arase, Y; Fujiyama, S; Hosaka, T; Ikeda, K; Kawamura, Y; Kobayashi, M; Kumada, H; Kuwano, T; Saitoh, S; Sezaki, H; Suzuki, F; Suzuki, Y1
Krause, S; Lochmüller, H; Müller-Felber, W; Müller-Höcker, J; Najmabadi, H; Pongratz, D; Schlotter-Weigel, B; Walter, MC; Wiendl, H1
Engel, AG; Fidzianska, A; Ryniewicz, B; Shen, XM1

Other Studies

3 other study(ies) available for valine and Inclusion Body Myopathy, Sporadic

ArticleYear
A Patient with HCV Infection and a Sustained Virological Response to Direct-acting Antiviral Treatment Who Developed Inclusion Body Myositis.
    Internal medicine (Tokyo, Japan), 2018, Sep-01, Volume: 57, Issue:17

    Topics: Aged; Anilides; Antiviral Agents; Carbamates; Cryoglobulinemia; Cyclopropanes; Female; Hepatitis C, Chronic; Humans; Lactams, Macrocyclic; Macrocyclic Compounds; Myositis, Inclusion Body; Proline; Ritonavir; Sulfonamides; Sustained Virologic Response; Valine

2018
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation.
    Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:10

    Topics: Adult; Carbohydrate Epimerases; Diagnosis, Differential; DNA Mutational Analysis; Genetic Predisposition to Disease; Histocompatibility Antigens Class I; Homozygote; Humans; Inflammation; Iran; Male; Muscle Fibers, Skeletal; Muscle, Skeletal; Mutation, Missense; Myositis, Inclusion Body; Pedigree; Valine

2003
IBM-type inclusions in a patient with slow-channel syndrome caused by a mutation in the AChR epsilon subunit.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:11

    Topics: Acetylcholine; Adult; Bungarotoxins; Cell Line; DNA Mutational Analysis; Dose-Response Relationship, Drug; Female; Humans; Iodine Isotopes; Membrane Potentials; Microscopy, Electron, Transmission; Molecular Sequence Data; Muscle, Skeletal; Mutation; Myasthenic Syndromes, Congenital; Myositis, Inclusion Body; Patch-Clamp Techniques; Protein Binding; Radioligand Assay; Receptors, Nicotinic; Transfection; Valine

2005